| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7874161-7874471 | Common:1; Rare:74 | ||||
| chr19:7903462-7903852 | Common:2; Rare:129 | ||||
| chr19:7920154-7920382 | Rare:81 | ||||
| chr19:7925471-7925735 | Common:2; Rare:70 | ||||
| chr19:7943632-7944030 | Rare:119 | ||||
| chr19:8005481-8005825 | Common:1; Rare:120 | ||||
| chr19:8307977-8308143 | Common:3; Rare:56; Clinvar (benign):1 | ||||
| chr19:8308271-8308669 | Common:4; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:8321290-8321703 | Common:2; Rare:164 | ||||
| chr19:8390032-8390431 | Common:2; Rare:111 | ||||
| chr19:8444787-8445118 | Common:4; Rare:145; Clinvar (benign):1 | ||||
| chr19:8514087-8514274 | Common:2; Rare:54 | ||||
| chr19:8526319-8526484 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr19:8832172-8832340 | Rare:60 | ||||
| chr19:9140304-9140446 | Common:2; Rare:40 |